ADVIL ALLERGY CONGESTION RELIEF- chlorpheniramine maleate, ibuprofen, and phenylephrine hydrochloride tablet, coated

Advil Allergy Congestion Relief by

Drug Labeling and Warnings

Advil Allergy Congestion Relief by is a Otc medication manufactured, distributed, or labeled by Select Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients (in each tablet)	Purposes
* nonsteroidal anti-inflammatory drug
Chlorpheniramine maleate 4 mg	Antihistamine
Ibuprofen 200 mg (NSAID)*	Pain reliever/Fever reducer
Phenylephrine HCl 10 mg	Nasal decongestant

Uses

• temporarily relieves these symptoms associated with hay fever or other upper respiratory allergies, and the common cold:
  • runny nose
  • itchy, watery eyes
  • itching of the nose or throat
  • sneezing
  • nasal congestion
  • sinus pressure
  • headache
  • minor body aches and pains
  • fever
• reduces swelling of the nasal passages
• temporarily restores freer breathing through the nose

Warnings

Allergy alert

Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:

• hives
• facial swelling
• asthma (wheezing)
• shock
• skin reddening
• rash
• blisters

If an allergic reaction occurs, stop use and seek medical help right away.

Stomach bleeding warning

This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:

• are age 60 or older
• have had stomach ulcers or bleeding problems
• take a blood thinning (anticoagulant) or steroid drug
• take other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others]
• have 3 or more alcoholic drinks every day while using this product
• take more or for a longer time than directed

Heart attack and stroke warning

NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

Do not use

• in children under 12 years of age because this product contains too much medication for children under this age
• if you have ever had an allergic reaction to any other pain reliever/fever reducer
• right before or after heart surgery
• if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product

Ask a doctor before use if

• you have a breathing problem such as emphysema or chronic bronchitis
• stomach bleeding warning applies to you
• you have problems or serious side effects from taking pain relievers or fever reducers
• you have a history of stomach problems, such as heartburn
• you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, thyroid disease, diabetes, glaucoma, have trouble urinating due to an enlarged prostate gland, or had a stroke
• you are taking a diuretic

Ask a doctor or pharmacist before use if you are

• under a doctor's care for any serious condition
• taking sedatives or tranquilizers
• taking any other product that contains phenylephrine, chlorpheniramine or any other nasal decongestant or antihistamine
• taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
• taking any other drug

When using this product

• take with food or milk if stomach upset occurs
• avoid alcoholic drinks
• be careful when driving a motor vehicle or operating machinery
• drowsiness may occur
• alcohol, sedatives, and tranquilizers may increase drowsiness
• may cause excitability especially in children

Stop use and ask a doctor if

• you experience any of the following signs of stomach bleeding:
  • feel faint
  • vomit blood
  • have bloody or black stools
  • have stomach pain that does not get better
• you have symptoms of heart problems or stroke:
  • chest pain
  • trouble breathing
  • weakness in one part or side of body
  • slurred speech
  • leg swelling
• pain gets worse or lasts more than 7 days
• fever gets worse or lasts more than 3 days
• nasal congestion lasts for more than 7 days
• redness or swelling is present in the painful area
• you get nervous, dizzy, or sleepless
• symptoms continue or get worse
• any new symptoms appear

If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use ibuprofen during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

• do not take more than directed
• adults and children 12 years of age and over:
  • take 1 tablet every 4 hours while symptoms persist
  • do not take more than 6 tablets in any 24-hour period, unless directed by a doctor
• children under 12 years of age: do not use because this product contains too much medication for children under this age

Other information

• read all warnings and directions before use. Keep card.
• store at 20-25°C (68-77°F)
• avoid excessive heat above 40°C (104°F)

Inactive ingredients

acesulfame potassium, artificial flavors, carnauba wax, colloidal silicon dioxide, corn starch, croscarmellose sodium, glycerin, glyceryl dibehenate, hypromellose, lactic acid, lecithin, maltodextrin, medium-chain triglycerides, microcrystalline cellulose, pharmaceutical ink, polydextrose, polyvinyl alcohol, pregelatinized starch, propyl gallate, silicon dioxide, sucralose, synthetic iron oxide, talc, titanium dioxide, triacetin, xanthan gum

Questions or comments?

Call weekdays from 9 AM to 5 PM EST toll free at 1-800-88-ADVIL

SPL UNCLASSIFIED SECTION

Product Repackaged and Distributed
with permission of Pfizer Consumer Healthcare by:
Select Corporation Carrollton, TX 75007

PRINCIPAL DISPLAY PANEL - 1 Tablet Pouch Blister Pack

Advil®

ALLERGY & CONGESTION RELIEF

Chlorpheniramine Maleate 4 mg Antihistamine
Ibuprofen 200 mg Pain Reliever/Fever Reducer (NSAID)
Phenylephrine HCl 10 mg Nasal Decongestant

1 PILL
DOSAGE

Relief of: Sinus Pressure, Nasal Swelling &
Congestion, Sneezing, Runny Nose and Headache

1
COATED
TABLET

INGREDIENTS AND APPEARANCE

ADVIL ALLERGY CONGESTION RELIEF 
chlorpheniramine maleate, ibuprofen, and phenylephrine hydrochloride tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52904-787(NDC:0573-0196)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chlorpheniramine maleate (UNII: V1Q0O9OJ9Z) (Chlorpheniramine - UNII:3U6IO1965U)	Chlorpheniramine maleate	4 mg
Ibuprofen (UNII: WK2XYI10QM) (Ibuprofen - UNII:WK2XYI10QM)	Ibuprofen	200 mg
Phenylephrine hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV)	Phenylephrine hydrochloride	10 mg

Inactive Ingredients
Ingredient Name	Strength
acesulfame potassium (UNII: 23OV73Q5G9)
carnauba wax (UNII: R12CBM0EIZ)
silicon dioxide (UNII: ETJ7Z6XBU4)
STARCH, CORN (UNII: O8232NY3SJ)
croscarmellose sodium (UNII: M28OL1HH48)
glycerin (UNII: PDC6A3C0OX)
glyceryl dibehenate (UNII: R8WTH25YS2)
hypromellose, unspecified (UNII: 3NXW29V3WO)
lactic acid, unspecified form (UNII: 33X04XA5AT)
egg phospholipids (UNII: 1Z74184RGV)
maltodextrin (UNII: 7CVR7L4A2D)
medium-chain triglycerides (UNII: C9H2L21V7U)
microcrystalline cellulose (UNII: OP1R32D61U)
polydextrose (UNII: VH2XOU12IE)
polyvinyl alcohol, unspecified (UNII: 532B59J990)
propyl gallate (UNII: 8D4SNN7V92)
sucralose (UNII: 96K6UQ3ZD4)
ferric oxide red (UNII: 1K09F3G675)
talc (UNII: 7SEV7J4R1U)
titanium dioxide (UNII: 15FIX9V2JP)
triacetin (UNII: XHX3C3X673)
xanthan gum (UNII: TTV12P4NEE)

Product Characteristics
Color	GRAY	Score	no score
Shape	OVAL	Size	17mm
Flavor		Imprint Code	Advil;A;CR
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52904-787-03	1 in 1 BLISTER PACK	07/23/2012
1		2 in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 52904-787-04	2 in 1 BLISTER PACK	07/23/2012
2		1 in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 52904-787-25	25 in 1 CARTON	07/23/2012
3		1 in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 52904-787-50	50 in 1 CARTON	07/23/2012
4		1 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part343	07/23/2012

Labeler - Select Corporation (053805599)